Retinal Disorder

Ophthalmic 131 variants 29 genes

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Associated Genes (29)

PRPH2 COQ8B GUCY2D USH2A RPGR ABCA4 IFT140 SSBP1 MERTK TSPAN12 CTC1 ADAMTS18 ACBD5 MYO7A CEP290 RP2 MFSD8 TRPM1 CACNA1F EYS NBAS HGSNAT RP1 PROM1 BEST1 GPR143 CFAP410 PCARE ADGRV1

Associated Variants (131)

RSID	Gene	Risk Allele	Odds Ratio	Evidence
RS370994796	PRPH2	—	—	strong
RS113358395	COQ8B	—	—	strong
RS61750171	GUCY2D	—	—	strong
RS41314534	USH2A	—	—	strong
RS1569237077	RPGR	—	—	strong
RS552517556	ABCA4	—	—	strong
RS770731272	IFT140	—	—	strong
RS745654673	ABCA4	—	—	strong
RS1662208035	ABCA4	—	—	strong
RS1975743813	GUCY2D	—	—	strong
RS1799747454	SSBP1	—	—	strong
RS1191143782	ABCA4	—	—	strong
RS745461381	MERTK	—	—	strong
RS781223647	USH2A	—	—	strong
RS1283326178	TSPAN12	—	—	strong
RS779499831	CTC1	—	—	strong
RS139516327	ADAMTS18	—	—	strong
RS200849015	ABCA4	—	—	strong
RS1426447692	ACBD5	—	—	strong
RS568495838	MYO7A	—	—	strong
RS2152010923	PRPH2	—	—	strong
RS746413821	CEP290	—	—	strong
RS1325681486	USH2A	—	—	strong
RS2523624821	ABCA4	—	—	strong
RS2519918569	RP2	—	—	strong
RS757641323	CEP290	—	—	strong
RS150418024	MFSD8	—	—	strong
RS369742878	TRPM1	—	—	strong
RS794726979	ABCA4	—	—	strong
RS797044676	CACNA1F	—	—	strong
RS794727631	EYS	—	—	strong
RS753330544	USH2A	—	—	strong
RS759315662	NBAS	—	—	strong
RS112029032	HGSNAT	—	—	strong
RS200692438	ABCA4	—	—	strong
RS878853328	RP1	—	—	strong
RS749526785	ABCA4	—	—	strong
RS543698823	PROM1	—	—	strong
RS281865265	BEST1	—	—	strong
RS1057518164	GPR143	—	—	strong
RS1057518955	ABCA4	—	—	strong
RS199740930	EYS	—	—	strong
RS753886165	USH2A	—	—	strong
RS140451304	CFAP410	—	—	strong
RS770553471	USH2A	—	—	strong
RS201238640	USH2A	—	—	strong
RS749228276	USH2A	—	—	strong
RS367658438	PCARE	—	—	strong
RS747323414	CEP290	—	—	strong
RS1307312865	ADGRV1	—	—	strong

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